US6060454A - Compositions, apparatus and methods for facilitating surgical procedures - Google Patents

Compositions, apparatus and methods for facilitating surgical procedures Download PDF

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US6060454A
US6060454A US09/131,075 US13107598A US6060454A US 6060454 A US6060454 A US 6060454A US 13107598 A US13107598 A US 13107598A US 6060454 A US6060454 A US 6060454A
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blocker
heart
administered
carbachol
node
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Francis G. Duhaylongsod
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Duke University
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Duke University
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Assigned to DUKE UNIVERSITY reassignment DUKE UNIVERSITY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DUHAYLONGSOD, FRANCIS G.
Priority to US09/379,180 priority patent/US6043273A/en
Priority to US09/382,705 priority patent/US6141589A/en
Priority to US09/379,179 priority patent/US6127410A/en
Priority to US09/379,381 priority patent/US6087394A/en
Priority to US09/406,333 priority patent/US6711436B1/en
Priority to US09/469,956 priority patent/US6101412A/en
Priority to US09/494,145 priority patent/US6414018B1/en
Publication of US6060454A publication Critical patent/US6060454A/en
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/27—Esters, e.g. nitroglycerine, selenocyanates of carbamic or thiocarbamic acids, meprobamate, carbachol, neostigmine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
    • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
    • A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2210/00—Anatomical parts of the body
    • A61M2210/12—Blood circulatory system
    • A61M2210/125—Heart

Definitions

  • the present invention relates to compositions and methods that facilitate the performance of medical and surgical procedures, such as cardiac surgical procedures, including minimally invasive coronary bypass surgery.
  • Heart attacks and angina pectoris are caused by occlusions in the coronary arteries.
  • Atherosclerosis the major cause of coronary artery occlusions, is characterized by deposits of fatty substances, cholesterol, calcium and fibrin within the arterial wall.
  • myocardial ischemia Severe and prolonged myocardial ischemia produces irreparable damage to the heart muscle, pronounced cardiac dysfunction, and possibly death.
  • CABG coronary artery bypass graft surgery
  • PTCA percutaneous transluminal coronary angioplasty
  • stents atherectomy
  • TMLR transmyocardial laser revascularization
  • CABG cardiopulmonary bypass
  • the hyperkalemic cardioplegic solution protects the heart by stopping atrial and ventricular contraction, thereby reducing its metabolic demand.
  • blood flow to the rest of the body is provided by means of CPB.
  • Cardiopulmonary bypass involves removing deoxygenated blood through the cannula in the right atrium, infusing the blood with oxygen, and then returning it through the cannula in the aorta to the patient.
  • the surgeon augments blood flow to the ischemic heart muscle by redirecting blood around the coronary artery occlusion.
  • LITA left internal thoracic artery
  • the LITA normally originates from the left subclavian artery and courses along the anterior chest wall just lateral of the sternum. For this operation, the LITA is mobilized from the chest wall and, with its proximal origin left intact, the distal end is divided and sewn to the coronary artery beyond the site of occlusion (most commonly the left anterior descending coronary artery). After the LITA anastomosis is completed and any further arterial or vein grafts are completed, CPB is weaned as the heart resumes its normal rhythm. The cannulae are removed, temporary pacing wires are sewn to the heart, and plastic tubes are passed through the chest wall and positioned near the heart to drain any residual fluid collection. The two halves of the sternum are approximated using steel wire.
  • the port-access approach avoids the sternal splitting incision by employing femoral venoarterial CPB and an intraaortic (endoaortic) balloon catheter that functions as an aortic clamp by means of in expandable balloon at its distal end
  • femoral venoarterial CPB and an intraaortic (endoaortic) balloon catheter that functions as an aortic clamp by means of in expandable balloon at its distal end
  • This catheter also includes a separate lumen for the delivery of cardioplegic solution and venting of the aortic root.
  • a different catheter may be placed percutaneously into the internal jugular vein and positioned in the coronary sinus for delivery of retrograde cardioplegic solution.
  • Coronary bypass grafting is performed through a separate limited left anterior thoracotomy incision with dissection of the LITA and anastomosis to the atherosclerotic coronary artery under direct vision.
  • the port-access approach does not avoid the damaging effects of cardiopulmonary bypass, which include: 1) a systemic inflammatory response; 2) interstitial pulmonary edema; 3) neuropsychological impairment; 4) acute renal insufficiency; and 5) nonmechanical microvascular hemorrhage.
  • the MIDCAB approach also avoids the sternal splitting incision, favoring instead a limited left anterior thoracotomy incision (Tea E. Acuff et al. "Minimally Invasive Coronary Artery Bypass Grafting.” Annals of Thoracic Surgery 1996; 61:135-7. Federico J. Benetti and Carlos Ballester, "Use Of Thoracoscopy And A Minimal Thoracotomy, In Mammary-Coronary Bypass To Left Anterior Descending Artery, Without Extracorporeal Circulation.” Journal of Cardiovascular Surgery 1995; 36:159-61. Federico J. Benetti et al. "Video Assisted Coronary Bypass Surgery.” Journal of Cardiac Surgery 1995; 10:620-625).
  • MIDCAB compared to conventional CABG
  • the potential advantages of MIDCAB compared to conventional CABG include: 1) the avoidance of CPB and aortic cross-clamping; 2) fewer embolic strokes; 3) less blood loss, hence a decreased transfusion requirement; 4) fewer perioperative supraventricular arrhythmias; 5) earlier separation from mechanical ventilatory support; 6) decreased or eliminated intensive care unit stay; 7) shorter length of hospitalization; 8) reduced total convalescence with earlier return to preoperative activity level; and 9) lower overall cost.
  • the durability of the LITA to coronary artery anastomosis is uncertain.
  • the Mayo Clinic group reported on 15 patients undergoing MIDCAB.
  • port-access and minimally invasive direct coronary artery bypass techniques avoid the operative trauma and morbidity associated with the sternal splitting incision, both have serious disadvantages.
  • the port-access approach is encumbered by the morbidity of cardiopulmonary bypass and aortic cross-clamping and the cost of the apparatus.
  • the safety of the intraaortic balloon clamp and the vascular sequelae of groin cannulation are unresolved issues.
  • the MIDCAB approach is imperiled by the constant motion of the beating heart which precludes a precise coronary anastomosis. Reports of poor graft patency rates and the need for early reoperation in a significant proportion of patients after MIDCAB attests to the technical difficulty of the procedure.
  • Potassium impedes excitation-contraction coupling, however, making it impossible to pace the heart by electrical stimulation and necessitating the use of a cardiopulmonary bypass system to sustain the patient.
  • Other chemical agents that have been used in human cardiac operations to slow the rate of ventricular contraction include acetylcholine, neostigmine, adenosine, lignocaine, and esmolol.
  • Another agent, carbachol or carbamyl choline has been used to induce cardiac arrest in experimental animals. Broadley and Rothaul, Pflugers Arch., 391:147-153 (1981).
  • Acetylcholine has been used as a cardioplegic agent during cardiopulmonary bypass.
  • Lam et al. "Induced Cardiac Arrest In Intracardiac Procedures, An Experimental Study," Journal of Thoracic Surgery 1955; 30:620-25; Lam et al., “Clinical Experiences With Induced Cardiac Arrest During Intracardiac Surgical Procedures," Annals of Surgery 1957; 146:439-49; Lam et al., “Induced Cardiac Arrest (Cardioplegia) In Open Heart Procedures," Surgery 1958; 43:7-13; and Lam et al., "Acetylcholine-induced Asystole.
  • Ventricular asystole has been achieved by direct injection of lignocaine into the interventricular septum. Khanna and Cullen, "Coronary Artery Surgery With Induced Temporary Asystole And Intermittent Ventricular Pacing: An Experimental Study," Cardiovascular Surgery 1996; 4(2):231-236. Epicardial pacing wires were placed, and ventricular pacing was employed to maintain an adequate cardiac output. Esmolol has been used as a cardioplegic agent during cardiopulmonary bypass. Mauricio Ede et al., “Beyond Hyperkalemia: Beta-Blocker-Induced Cardiac Arrest For Normothermic Cardiac Operations," Annals of Thoracic Surgery, 1997; 63:721-727.
  • Methods, compositions and apparatus are provided which are useful for medical and surgical therapeutic applications.
  • the methods and compositions are useful for cardiac surgery and other procedures, such as neurosurgery and vascular surgery, which require precise control of cardiac contraction.
  • Other applications include non-invasive procedures such as percutaneous aortic aneurysm graft placement, and invasive procedures such as brain surgery.
  • a substantially motionless operative field is provided.
  • a method of inducing reversible ventricular asystole in a beating heart in a human patient comprising administering a compound and a ⁇ -blocker to the heart of the patient in an amount effective to induce ventricular asystole, while maintaining the ability of the heart to be electrically paced, wherein the ⁇ -blocker is administered in amount sufficient to substantially reduce the amount of compound required to induce ventricular asystole.
  • the compound may be an atrioventricular (AV) node blocker.
  • the ⁇ -blocker may be administered in an amount sufficient to reduce the amount of AV node blocker, which is required to induce ventricular asystole, to, for example, about 50% or less by weight of the amount of AV node blocker alone required to induce ventricular asystole.
  • the compound may be a cholinergic receptor agonist, such as carbachol.
  • the cholinergic receptor agonist, such as carbachol may be administered in an amount, for example, of about 0.1 to 4.8 ⁇ g/kg body weight/min.
  • the ⁇ -blocker may be, for example, propranolol.
  • the propranolol may be administered, for example, in an amount of about 0.01 to 0.07 mg/kg body weight.
  • the ⁇ -blocker is propranolol and the AV node blocker is carbachol, and the propranolol is administered prior to or during administration of the carbachol.
  • the propranolol and the carbachol may be administered, for example, to the coronary artery of the patient.
  • a method of inducing reversible ventricular asystole in a beating heart in a human patient comprising administering a cholinergic receptor agonist and a ⁇ -blocker to the heart of the patient in an amount effective to induce ventricular asystole, wherein the amount administered of the cholinergic receptor agonist alone or the ⁇ -blocker alone is not sufficient to induce ventricular asystole.
  • a method of conducting a surgical procedure on a human patient comprising: administering a ⁇ -blocker and an AV node blocker to the heart of a human patient to induce reversible ventricular asystole while maintaining the ability of the heart to be electrically paced; electrically pacing the heart with an electrical pacing system; selectively intermittently stopping the electrical pacing to allow ventricular asystole; and conducting the surgical procedure during the time that the electrical pacing is intermittently stopped.
  • the ⁇ -blocker is administered prior to the AV node blocker.
  • the AV node blocker may be a cholinergic agent, such as carbachol.
  • the ⁇ -blocker may be administered in an amount sufficient to substantially reduce the amount of AV node blocker required to induce ventricular asystole.
  • the surgical procedure may be, for example, a cardiac surgical procedure.
  • the electrical pacing is selectively intermittently interrupted by a surgeon conducting the surgical procedure by selectively manipulating a control that is functionally coupled to the electrical pacing system.
  • the ⁇ -blocker and the cholinergic agent may be administered, for example, sequentially or simultaneously, and may be administered, for example, to the right or left coronary artery, left ventricle, the aorta, the right ventricle, the pulmonary artery, the pulmonary vein, or the coronary sinus.
  • the cholinergic receptor agonist such as carbachol
  • the ⁇ -blocker may be, for example, propranolol, which may be administered, for example, in an amount of about 0.01 to 0.07 mg/kg body weight.
  • the ⁇ -blocker is propranolol and the AV node blocker is carbachol, and the propranolol is administered prior to or during administration of the carbachol.
  • the propranolol is administered by a single bolus injection in the right or left coronary artery, prior to the administration of carbachol, and the carbachol is administered by a single bolus injection followed by continuous infusion into the right or left coronary artery to maintain the ventricular asystole.
  • Surgical procedures that may be conducted include minimally invasive coronary bypass procedures, neurological procedures and endovascular procedures.
  • Other surgical procedures include treatment of injuries to the liver, spleen, heart, lungs, and major blood vessels, as well as electrophysiologic procedures and cardiac surgery with or without cardiopulmonary bypass.
  • a method of inducing reversible ventricular asystole in a human patient comprising administering carbachol to the heart of the patient.
  • the carbachol may be administered, for example, to the coronary sinus, or may be administered intraventricularly, or to the aortic root or coronary artery of the patient.
  • propranolol also may be administered to the heart of the patient. The propranolol may be administered, for example, prior to or during the administration of the carbachol.
  • a method of inducing reversible ventricular asystole in the heart of a human patient comprising administering carbachol to the patient at a dosage of about 1 to 15 mg, for example, about 1 to 12 mg.
  • a method of inducing reversible ventricular asystole in the heart of a human patient comprising administering carbachol to the patient at a rate of 0.1 to 4.8 ⁇ g/kg body weight/min.
  • a method of inducing reversible ventricular asystole in the heart of a human patient comprising: administering an initial intracoronary bolus of carbachol of about 0.1 to 10 ⁇ g/kg body weight of the patient; and administering a continuous intracoronary infusion of carbachol at a rate of about 0.1-4.8 ⁇ g/kg body weight/min.
  • the initial intracoronary bolus of carbachol is administered, for example, over about 1-5 minutes.
  • the intracoronary infusion of carbachol is administered, for example, over a time period of about 5 to 120 minutes.
  • the initial intracoronary bolus may comprise, for example about 0.1 to 5 ⁇ g carbachol/kg body weight, and may be provided in a suitable pharmaceutically acceptable carrier.
  • a method of inducing reversible ventricular asystole in a human patient comprising: administering an intracoronary bolus injection of about 0.01 to 0.5 mg of carbachol over about 0.5 to 3 minutes; and administering an intracoronary infusion of carbachol at a rate of about 0.01 to 0.3 mg/min over about 30 to 90 minutes.
  • a method of inducing reversible ventricular asystole of a heart of a human patient while maintaining the ability of the heart to be electrically paced comprising: administering at least a first compound to the heart of the patient which is capable of inducing third-degree AV block of the heart; and administering at least a second compound to the heart of the patient which alone or in combination with the first compound is capable of substantially suppressing ectopic ventricular beats in the heart while maintaining the ability of the heart to be electrically paced.
  • a method of inducing reversible ventricular asystole in the heart of a patient, while maintaining the ability of the heart to be electrically paced comprising: administering an AV-node blocker and a compound to the heart of the patient in an amount effective to induce ventricular asystole, while maintaining the ability of the heart to be electrically paced, wherein the compound is administered in an amount sufficient to reduce the amount of AV-node blocker required to induce ventricular asystole.
  • a method of performing a surgical procedure on a human patient comprising: administering an effective amount of a composition capable of inducing reversible ventricular asystole to the patient, while maintaining the ability of the heart to be electrically paced; electrically pacing the heart with an electrical pacing system, thereby to maintain the patient's blood circulation; selectively intermittently stopping the electrical pacing to allow ventricular asystole; and conducting the surgical procedure during the time that the electrical pacing is intermittently stopped.
  • the composition capable of inducing ventricular asystole may comprise, in one embodiment, an atrioventricular (AV) node blocker.
  • the composition may further comprise a ⁇ -blocker, wherein the ⁇ -blocker is present in an amount sufficient to substantially reduce the amount of AV node blocker required to induce ventricular asystole.
  • the composition may comprise a cholinergic agent and a ⁇ -blocker, wherein the amount by weight administered of either the cholinergic agent alone or the ⁇ -blocker alone is not sufficient to induce complete heart block and suppression of ventricular escape beats, but in combination, due to a synergistic effect, is effective to induce ventricular asystole.
  • a cardiac surgical procedure is conducted by inducing reversible ventricular asystole in the heart of a human patient without cardiopulmonary bypass, and/or without aortic cross-clamping.
  • a composition is provided that is capable of inducing reversible ventricular asystole in a patient, while maintaining the ability of the heart to be electrically paced.
  • the composition may include an atrioventricular (AV) node blocker.
  • the composition may include a compound capable of inducing reversible ventricular asystole in a patient and a ⁇ -blocker in an amount sufficient to substantially reduce the amount of the compound required to induce ventricular asystole in the patient.
  • the composition may include, for example, an atrioventricular (AV) node blocker, such as carbachol and a ⁇ -blocker, such as propranolol.
  • the ⁇ -blocker is provided in one embodiment in an amount sufficient to substantially reduce the amount of AV node blocker required to induce ventricular asystole.
  • the AV node blocker may be present in the composition in an amount which is 50% or less by weight, or optionally about 1 to 20% by weight of the amount of AV node blocker alone required to induce ventricular asystole.
  • the composition may comprise, for example carbachol in a pharmaceutically acceptable solution at a dosage amount of about 1 to 20 mg.
  • the comopsition may include propranolol in a pharmaceutically acceptable carrier in a dosage form for administration to a patient in an amount of about 0.01 to 0.07 mg/kg body weight of the patient.
  • the composition may comprise propranolol present in a pharmaceutically acceptable solution at a dosage amount of about 1 to 10 mg.
  • Methods are provided for administering an effective amount of the compositions to a patient to induce reversible ventricular asystole during a surgical procedure.
  • a composition which is capable of inducing ventricular asystole in a patient, while maintaining the ability of the heart to be electrically paced, comprising a cholinergic receptor agonist and a ⁇ -blocker.
  • the amount of either the cholinergic receptor agonist alone or the ⁇ -blocker alone in the composition is not sufficient to induce ventricular asystole in the patient.
  • a sterile dosage form of carbachol is provided, which may be provided in form suitable for use in a surgical procedure.
  • the dosage form of carbachol may be in a pharmaceutically acceptable form for parenteral administration, for example to the cardiovascular system, or directly to the heart, such as by intracoronary infusion.
  • the carbachol may be provided in a variety of pharmaceutically acceptable carriers.
  • a sterile dosage form of carbachol comprising about 1-20 mg of carbachol in a pharmaceutically acceptable carrier.
  • Carriers include aqueous solutions including saline, aqueous solutions including dextrose, water and buffered aqueous solutions.
  • the invention provides the use of a ⁇ -blocker in the manufacture of a medicament for use in conjunction with a compound capable of inducing reversible ventricular asystole in the heart of a patient, for use in a method of inducing transient reversible ventricular asystole in the heart of a patient, while maintaining the ability of the heart be electrically paced, the amount of ⁇ -blocker being sufficient to reduce substantially the amount of the compound required to induce ventricular asystole.
  • a ⁇ -blocker in the manufacture of a medicament for use in conjunction with a cholinergic receptor agonist, for use in a method of inducing transient reversible ventricular asystole in the heart of a patient, while maintaining the ability of the heart to be electrically paced, the amount of the cholinergic receptor agonist administered alone or the ⁇ -blocker administered alone not being sufficient to induce ventricular asystole in the heart of the patient.
  • a cholinergic receptor agonist in the manufacture of a medicament for use in conjunction with a ⁇ -blocker, for use in a method of inducing transient reversible ventricular asystole in the heart of a patient, while maintaining the ability of the heart to be electrically paced, the amount of cholinergic receptor agonist administered alone or the ⁇ -blocker administered alone not being sufficient to induce ventricular asystole in the heart of the patient.
  • a patient may be prepared for coronary artery bypass by placing at least a portion of a delivery device in a coronary vessel of the patient's heart and delivering a cardioplegic agent to the AV node of the patient via the coronary vessel with the device, which may be a catheter, for example.
  • the device is placed in the right coronary artery of the heart of the patient. In another embodiment, it is placed in the left coronary artery of the heart of the patient.
  • the device may include an outlet and the outlet placed in the right coronary artery of the heart of the patient and immediately proximal to the AV node artery. In another embodiment, the device outlet may be placed in the AV node artery.
  • the device may be placed in the middle cardiac vein of the heart of the patient or in an ostium of a right or left coronary artery of the heart of the patient.
  • the device may be introduced through the femoral artery.
  • the device also may be introduced through an incision in the aorta of the patient.
  • a kit comprising one or more agents capable of inducing ventricular asystole.
  • the kit may include separate containers of an AV node blocker and a ⁇ -blocker.
  • the kit is provided with a first container comprising a dosage amount of a cholinergic receptor agonist and a second container comprising a dosage amount of a ⁇ -blocker.
  • Dosage amounts of cholinergic receptor agonist and ⁇ -blocker may be included that are suitable for simultaneous, separate or sequential use in a surgical procedure for inducing transient reversible ventricular asystole in a patient.
  • the cholinergic receptor agonist is carbachol and the ⁇ -blocker is propranolol.
  • the carbachol and/or propranolol may be in a pharmaceutically acceptable carrier.
  • the first container contains about 1 to 20 mg of carbachol, and the second container contains about 1 to 10 mg of propranolol.
  • Other possible components of the kit include pacing electrodes, drug delivery devices and catheters.
  • the electrodes may be, for example, epicardial or endocardial pacing electrodes.
  • Other components of the kit can include pacing catheters and devices, and coronary perfusion catheters and devices, catheter introducers, a pump system and/or tubes, or other surgical devices.
  • the drug delivery device may be in various forms including a catheter, such as a drug delivery catheter or guide catheter, a cannula or a syringe and needle assembly.
  • the drug delivery catheter may include an expandable member, and a shaft having a distal portion, wherein the expandable member is disposed along the distal portion.
  • the expandable member may be a low-pressure balloon.
  • the kit may be in packaged combination, such as in a pouch, bag or the like.
  • the kit may further include instructions for the use of components of the kit in a surgical procedure, such as instructions for use of compounds to induce transient reversible ventricular asystole in the heart of a patient undergoing a surgical procedure.
  • a pacing system comprising an extracorporeal pacer for delivering pacing signals to a human heart, a switch coupled to the pacer, and a switch actuator arranged remote from the pacer.
  • the remote actuator may enhance procedure control when used, for example, during a surgical procedure.
  • the pacing system may include pacing leads coupled to the switch and adapted for coupling to the heart of the patient.
  • the switch may be remote from the pacer.
  • the actuator may be remote from the switch.
  • the actuator may take various forms.
  • the actuator may comprise a foot pedal and in another, it may comprise a needle holder.
  • An actuator override circuit also may be provided as well as indicators indicating various states of pacing.
  • FIG. 1 diagramatically shows a pacing system in accordance with the principles of the invention
  • FIGS. 1A and 1B are circuit diagrams of a control switch and an actuator used in the pacing system of FIG. 1;
  • FIG. 1C is a schematic representation of a control box according to the present invention.
  • FIG. 1D diagrammatically shows one outlet lead arrangement coupled to the heart of a patient
  • FIG. 1E diagrammatically shows another outlet lead arrangement coupled to the heart of a patient
  • FIG. 2 illustrates a drug delivery catheter prior to insertion into the coronary sinus in accordance with the invention
  • FIG. 2A is a sectional view of the catheter of FIG. 2 taken along line 2A--2A;
  • FIG. 3 illustrates placement of the distal end portion of the catheter of FIG. 2 in the coronary sinus
  • FIG. 3A is a sectional view of the distal portion of the catheter of FIG. 3;
  • FIG. 4 illustrates another coronary sinus catheter configuration
  • FIG. 5 depicts a drug delivery catheter positioned for intra-aortic drug delivery in accordance with the present invention
  • FIG. 6 illustrates a drug delivery catheter positioned for drug delivery local to the AV node branch in accordance with the present invention
  • FIG. 7 illustrates another embodiment of the catheter of FIG. 6 showing a curved distal end portion for directing fluid toward the AV node
  • FIG. 8 depicts the catheter of FIG. 7 with its bent distal end portion directed toward the AV node branch.
  • compositions and methods are provided which are useful for medical and surgical therapeutic applications.
  • the compositions and methods are useful for cardiac surgery and other procedures such as neurosurgery and vascular surgery which require precise control of cardiac contraction.
  • the compositions and methods are useful for coronary artery bypass procedures, with or without cardiopulmonary bypass. Using the methods and compositions for conducting a coronary artery bypass disclosed herein, a motionless operative field is provided.
  • the methods and compositions of the invention are useful for any procedure which requires controlled temporary complete heart block and suppression of ventricular escape beats.
  • procedures include coronary bypass surgery (with full or partial sternotomy or thoracotomy), transmyocardial laser revascularization, tachyarrhythmia operations such as electrophysiology lab procedures (diagnostic and therapeutic ablation of arrhythmias), imaging procedures of the heart and great vessels such as CAT scan or MRI procedures, percutaneous transluminal coronary angioplasty, placement of stents such as coronary or aortic stents, operations where uncontrollable hemorrhage is present or anticipated or control of significant hemorrhage is required during the surgical procedure (for example, treatment of injuries to the liver, spleen, heart, lungs, or major blood vessels, including iatrogenic and traumatic injuries to such organs or structures), other procedures including percutaneous aortic aneurysm graft placement, and neurosurgical procedures, such as aneurysm repair.
  • compositions and methods can be used to induce ventricular asystole in a patient, for example, prior to a surgical procedure.
  • ventricular asystole refers to a state wherein autonomous electrical conduction and escape rhythms in the ventricle are suppressed.
  • a state of the heart is induced wherein the heart beats less than about 25 beats per minute, for example, less than about 12 beats per minute.
  • the induced ventricular asystole is reversible and after reversal, the heart functions are restored, and the heart is capable of continuing autonomous function.
  • pharmaceutically acceptable compositions which are capable of inducing transient reversible ventricular asystole reliably and predictably.
  • compositions capable of suppressing autonomous ventrical electrical conduction and escape rhythms may in one embodiment comprise an atrioventricular (AV) node blocker.
  • AV node blocker refers to a compound capable of reversibly suppressing autonomous electrical conduction at the AV node, while still allowing the heart to be electrically paced to maintain cardiac output.
  • the AV node blocker, or composition comprising the AV node blocker reduces or blocks ventricular escape beats and cardiac impulse transmission at the AV node of the heart, while the effect on depolarization of the pacemaker cells of the heart is minimal or non-existent.
  • the AV node blocker preferably induces third degree, or complete AV block, or significantly slows AV conduction to the point where the ventricular beat is less than about 25 beats per minute, for example less than about 12 beats per minute.
  • the AV node blocker, or composition comprising the AV node blocker preferably induces reversible ventricular asystole, and renders the heart totally pacemaker dependent for a limited period of time, such that a pacemaker may be used to maintain pacing and to intermittently stop pacing during a surgical step. After the surgical procedure is completed, for example, less than about 2 hours, the heart then can be returned to its normal intrinsic rhythm.
  • Exemplary AV node blockers include calcium channel blockers, adenosine A1 receptor agonists, adenosine deaminase inhibitors, cholinesterase inhibitors, monoamine oxidase inhibitors, serotoninergic agonists, antiarrythmics, cardiac glycosides, local anesthetics and combinations thereof.
  • AV node blockers examples include adenosine, digoxin, digitalis, procaine, lidocaine, procainamide, quinidine, verapamil, chloroquine, amiodarone, ethmozine, propafenone, flecainide, encainide, pilocarpine, diltazem, dipyridamole, ibutilide, zapranest, sotalol and metoclopromide and combinations thereof.
  • AV node blocking also can be achieved by other methods including direct electrical stimulation, vagal nerve stimulation, stimulation with ultrasonic energy, and temporary cooling of the AV node using a cryonic agent.
  • Cryonic agents include devices, such as cryostats, and cryogenic chemicals which are capable of inducing low temperatures at the AV node.
  • the AV node blocker capable of causing ventricular asystole, in a preferred embodiment is a cholinergic agent.
  • cholinergic agent refers to a cholinergic receptor modulator, which is preferably an agonist.
  • the cholinergic agent in a preferred embodiment is carbachol (carbamyl choline chloride).
  • Other cholinergic agents which may be used include any naturally occurring cholinergic (acetylcholine) receptor agonists or synthetic derivatives.
  • Exemplary cholinergic agents include acetylcholine, methacholine, bethanechol, arecoline, norarecoline, pyridostigmine, neostigmine, and other agents that increase cyclic GMP levels by direct or indirect receptor stimulation.
  • compositions and methods are provided which are capable of slowing or preventing autonomous conduction of electrical impulses from the sinoatrial node to the ventricle, with suppression of escape beats in the AV node and the ventricle.
  • a state of the heart is induced wherein the heart beats less than about 25 beats per minute, for example, less than about 12 beats per minute.
  • ⁇ -adrenergic blocking agent also referred to as a " ⁇ -blocker”
  • ⁇ -blocker is defined as an agent which is capable of blocking ⁇ -adrenergic receptor sites.
  • the ⁇ -blocker is propranolol.
  • Other ⁇ -blockers which can be used include atenolol, acebutolol, labetalol, metoprolol, nadolol, oxprenolol, penbutolol, pindolol, sotalol and timolol.
  • exemplary ⁇ -blockers include celiprolol, betaxolol, bevantolol, bisoprolol, esmolol, alprenolol, carterolol, nadolol or teratolol, and mixtures thereof.
  • the ⁇ -blocker may be any naturally occurring or synthetic analogue capable of blocking ⁇ -adrenergic receptor sites.
  • reversible ventricular asystole in a beating heart in a human patient is induced by administering to a patient a composition capable of suppressing autonomous ventricular electrical conduction and escape rhythms.
  • the composition capable of inducing ventricular asystole may comprise a first compound capable of inducing ventricular asystole, such as an AV node blocker, and a ⁇ -blocker present in an amount sufficient to substantially reduce the amount of the compound required to induce ventricular asystole.
  • the combination of the compound, such as an AV node blocker together with the ⁇ -blocker provides a synergistic effect such that the amount of AV node blocker required to induce reversible ventricular asystole may be reduced in comparison to the amount of AV node blocker required alone.
  • ventricular asystole is induced in a beating heart in a human patient by administering a cholinergic receptor agonist and a ⁇ -blocker to the heart of the patient in an effective amount to induce ventricular asystole, wherein the amount administered of the cholinergic receptor agonist alone or the ⁇ -blocker alone is not sufficient to induce ventricular asystole.
  • the co-administration of the ⁇ -blocker with the cholinergic agent provides a synergistic effect, such that the amount of cholinergic agent which is administered to induce reversible ventricular asystole can be reduced.
  • Reversible ventricular asystole in the heart of a human patient thus may be induced by administration of an AV node blocker, or mixture of AV node blockers, to the heart of the patient.
  • Reversible ventricular asystole optionally is induced by administration of the combination of an AV node blocker, such as a cholinergic agent, and one or more ⁇ -blockers to the heart of the patient.
  • the ⁇ -blocker is preferably administered either prior to or contemporaneously with the AV node blocker.
  • the method further includes electrically pacing the heart with an electrical pacing system, thereby to maintain the patient's blood circulation; selectively intermittently stopping the electrical pacing to allow ventricular asystole; and conducting the surgical procedure during the intervals of time that the electrical pacing is intermittently stopped.
  • the method may be used, for example, in a cardiac surgical procedure.
  • Electrical pacing may be controlled by a surgeon conducting the surgical procedure by selectively manipulating a control that is functionally coupled to the electrical pacing system.
  • pacing of the heart may be implemented using a external pacemaker connected to the heart, and the pacemaker may be periodically deactuated, for example by way of a foot switch, to allow reversible ventricular asystole, thereby facilitating the performance of coronary artery bypass, with or without cardiopulmonary bypass, or other procedures elsewhere in the body of the patient.
  • the patient's heart is provided with ventricular pacing electrodes connected to an electrical pacing device, which is controlled by the surgeon.
  • a composition for example, comprising an AV node blocker and a ⁇ -blocker, then is administered to the patient to induce reversible ventricular asystole.
  • the surgeon then employs the pacing device to pace the heart and sustain the patient's circulation.
  • the surgeon intermittently stops the electrical pacing for a few seconds to place a single suture, and re-starts it after each successive suture, thus permitting a precise coronary anastomosis to be performed.
  • the ventricles (and/or atria) are electrically paced and maintain a normal cardiac output except for the brief periods of time that are required to accurately place a single suture in the coronary artery, preferably about 2 to 15 seconds, and more preferably about 2 to 5 seconds.
  • the rate and timing of ventricular contraction can be directly controlled.
  • the composition inducing ventricular asystole such as an AV node blocker in combination with a ⁇ -blocker or AV node blocker administered after a ⁇ -blocker, may be infused through a catheter placed into the right coronary artery.
  • the composition is delivered locally to the AV node of the heart upon which it acts via the AV node artery of the heart.
  • the composition is delivered to the right coronary artery which feeds blood to the AV node artery.
  • the right coronary artery is the main vessel supplying blood to the right side of the heart and to the AV node.
  • the first septal branch of the left anterior descending artery which originates from the left coronary artery may be the vessel which delivers blood to the AV node and can be selected as the delivery conduit for delivering the composition to the AV node.
  • other possible routes of administration to the AV node may include Kugel's artery and the right superior descending artery.
  • the composition is delivered to the right coronary artery or left coronary artery at a location near the bifurcation to the AV node artery and proximal to the right coronary artery's bifurcation into the posterior descending artery by any one of a number of drug delivery means, such as a drug delivery catheter suitably positioned within the right coronary artery.
  • Other methods of administration may be used including hypodermic needle injection into, for example, any of the vessels noted above which may supply blood to the AV node, such as the right coronary artery or the first septal branch.
  • Other methods of administration include needle injection into the aorta, needle injection directly into the AV node artery or the AV node itself, a transepicardial absorption pad, i.e., a myocardial patch which slowly releases the composition directly into the heart's myocardium, and for example, an intraoperative cannula or other similar guide introducer or sheath which can be surgically placed by a surgeon into the aorta or the ostium of a coronary vessel without the need for X-ray fluoroscopy.
  • a transepicardial absorption pad i.e., a myocardial patch which slowly releases the composition directly into the heart's myocardium
  • an intraoperative cannula or other similar guide introducer or sheath which can be surgically placed by a surgeon into the aorta or the ostium of a coronary vessel without the need for X-ray fluoroscopy.
  • the ventricle is electrically paced to maintain a stable rhythm and blood pressure.
  • the surgeon uses a convenient control means, such as a foot pedal or hand held actuator, as shown in FIG. 1, and is thereby able to stop the heart as sutures are placed in the coronary arterial wall.
  • the time required to place a single suture into the coronary artery preferably does not exceed 15 seconds, and is preferably about 2 to 5 seconds, most preferably about 2 to 4 seconds.
  • the compositions can permit the elimination of the translational motion of the beating heart.
  • compositions capable of inducing ventricular asystole in a patient which in one embodiment include a cholinergic receptor agonist and a ⁇ -blocker, wherein the amount of the cholinergic receptor agonist alone or the ⁇ -blocker alone in the composition is not sufficient to induce ventricular asystole in the patient.
  • Methods are provided wherein the cholinergic receptor agonist and the ⁇ -blocker may be administered, either sequentially or together, thereby to induce ventricular asystole in a patient, wherein the amount of the cholinergic receptor agonist administered alone or the ⁇ -blocker administered alone is not sufficient to induce ventricular asystole in the patient.
  • a continuous infusion rate of about 0.1 to 4.8 ⁇ g/kg/min of carbachol can be used, e.g., an infusion rate of carbachol of 0.1 to 2.1 ⁇ g/kg/min, or about 0.1 to 1.5 ⁇ g/kg/min, or in one preferred embodiment, about 1.5 to 2.1 ⁇ g/kg/min.
  • the ratio by weight of propranolol to carbachol in the bolus injections can range, for example, from about 1:2 to 35:1, or, in another embodiment, from about 1:1 to 15:1, or, in another embodiment, from about 2:1 to 10:1, or, in another embodiment, is about 5:1.
  • compositions capable of inducing ventricular asystole in a patient comprising a compound, such as an atrioventricular (AV) node blocker, and a ⁇ -blocker, wherein the ⁇ -blocker is present in an amount sufficient to substantially reduce the amount of the compound required to induce ventricular asystole in the patient.
  • AV node blocker is preferably a cholinergic agent.
  • the cholinergic agent may be present in the composition in a reduced amount which is, for example, about 1-90%, about 1-50%, or about 1-20%, or for example, about 2-14%, or in another embodiment about 80% or less, for example about 50% or less, or about 10% or less by weight of the amount of the cholinergic agent alone required to induce ventricular asystole in the patient.
  • the co-administration of the ⁇ -blocker with the AV node blocker provides a synergistic effect, such that the amount of AV node blocker which is administered to induce ventricular asystole may be reduced.
  • ventricular asystole may be induced in a patient by administration, together, or sequentially, of a compound, such as an AV node blocker, together with a ⁇ -blocker, wherein the ⁇ -blocker is administered in an amount sufficient to substantially reduce the amount of the compound required to induce ventricular asystole in the patient.
  • the compound is a cholinergic agent, such as carbachol.
  • the cholinergic agent may be administered in reduced amount which is, for example, about 1-90%, about 1-50%, or about 1-20%, or in one embodiment, about 2-14%, or in another embodiment about 80% or less, about 50% or less, or about 10% or less by weight of the amount of the cholinergic agent alone required to induce ventricular asystole in the patient.
  • the ⁇ -blocker may be present in combination with other compounds capable of inducing ventricular asystole, in an amount effective to reduce the amount of the compound required to induce ventricular asystole, for example to about 5-90%, e.g., 30-50% or less by weight of the amount alone required to induce ventricular asystole.
  • the administration of the ⁇ -blocker is preferably prior to, or contemporaneously with, the administration of the cholinergic agent, and in one embodiment results in a synergistic effect between the ⁇ -blocker and the cholinergic agent.
  • the amount of ⁇ -locker present is preferably not sufficient to induce ventricular asystole by itself, and is sufficient only to cause a local ⁇ -blockade, but has a minimal effect on electrical conduction of the heart, or is low enough to cause only a first degree heart block.
  • an AV node blocker in order to induce reversible ventricular asystole in the heart of a patient, while maintaining the ability of the heart to be electrically paced, is administered in combination with an effective amount of a second compound, such as a ⁇ -blocker to reduce or suppress ectopic ventricular activity while maintaining the ability of the heart to be electrically paced.
  • a second compound such as a ⁇ -blocker to reduce or suppress ectopic ventricular activity while maintaining the ability of the heart to be electrically paced.
  • the ⁇ -blocker alone or in combination with the AV node blocker, is capable of substantially suppressing ectopic ventricular beats in the heart while maintaining the ability of the heart to be electrically paced.
  • an AV node blocker such as an antiarrythmic, such as flecainide
  • a ⁇ -blocker such as propranolol
  • the ⁇ -blocker is administered prior to the AV node blocker.
  • a composition is provided that includes an AV node blocker and a ⁇ -blocker in an amount effective to induce reversible ventricular asystole and wherein the ⁇ -blocker is present in an amount effective to reduce or suppress ectopic ventricular activity after administration.
  • a cholinergic agent such as carbachol
  • a ⁇ -blocker such as propranolol
  • a preferred half-life is on the order of about one to ten minutes.
  • a preferred onset of effect is less than one minute after administration. It is possible to induce onset of ventricular asystole within about thirty seconds after administration of carbachol and propranolol to the heart.
  • compositions preferably are capable of inducing reversible transient ventricular asystole of a beating heart to facilitate the performance of minimally invasive surgical procedures, while still permitting the heart to be electrically paced.
  • the compositions including for example a cholinergic agent, preferably can reliably and in a dose-dependent fashion produce extended periods of reversible ventricular asystole, for example, for up to about two hours upon either administration of a single dose, or continuous infusion, depending upon the composition.
  • the ventricular asystole is chemically reversible.
  • the ventricular asystole can be reversed by administering atropine, for example by an intravenous bolus injection, providing an important advantage of safety during the procedure.
  • the ⁇ -blocker is administered to the heart before the cholinergic agent.
  • the ⁇ -blocker in one embodiment is administered in a single bolus injection into the right or left coronary artery, and then the cholinergic agent is administered by a single bolus injection followed by continuous infusion into the right or left coronary artery throughout the surgical procedure, to maintain the ventricular asystole.
  • the ⁇ -blocker may be administered by continuous infusion, or a plurality of bolus infusions. The ventricular asystole continues as long as administration of the cholinergic agent is continued.
  • the ⁇ -blocker due to the prior administration of the ⁇ -blocker, it is possible to administer a significantly reduced amount of the cholinergic agent and thereby reduce the occurrence of side-effects such as systemic hypotension. Moreover, depolarization of the pacemaker cells of the heart by the administered composition is preserved, thereby making it possible to selectively electrically pace the heart to permit the performance of a surgical procedure while the heart is under transient ventricular asystole.
  • the time between administration of the ⁇ -blocker and the cholinergic agent is preferably long enough to permit the ⁇ -blocker to cause a local ⁇ -blockade of the pacemaker cells of the heart.
  • the time interval can be, for example about two minutes. In the case of intravenous or other forms of administration, several minutes or even hours may be required to permit the ⁇ -blocker to affect the pacemaker cells of the heart.
  • the subsequent administration of the cholinergic agent may be controlled by the surgeon.
  • Bolus infusion of higher doses can be used to give a dose dependent effect, while continuous infusion of lower doses also may be given to maintain ventricular asystole.
  • the ⁇ -blocker may be administered by an initial intracoronary bolus followed by a continuous infusion.
  • the AV node blocker such as a cholinergic agent, such as carbachol
  • a cholinergic agent such as carbachol
  • the AV node blocker, such as carbachol is preferably administered over a time period of about 0.1 to 3 minutes, preferably about 0.5 to 1 minute.
  • the AV node blocker such as a cholinergic agent, such as carbachol
  • a cholinergic agent such as carbachol
  • the bolus infusion of the AV node blocker such as a cholinergic agent is in one embodiment followed by a continuous intracoronary infusion at about 0.1-5 ⁇ g/kg body weight/min of the AV node blocker, which in a preferred embodiment is a cholinergic agent.
  • the infusion rate in one embodiment is about 0.1-4.8 ⁇ g/kg body weight of patient/min, for example about 0.1-2.1 ⁇ g/kg/min, or about 0.1-1.5 ⁇ g/kg/min, or about 0.1-1.0 ⁇ g/kg/min, or in another embodiment, about 0.1-0.5 ⁇ g/kg/min.
  • the cholinergic agent is combined with a ⁇ -blocker.
  • a typical total adult dosage of an AV node blocker such as a cholinergic agent, such as carbachol
  • This dosage can produce reversible ventricular asystole, for example, for a time period of about 5 to 120 minutes, for example, about 5 to 90 minutes, preferably about 30 to 90 minutes, e.g., about 75 minutes.
  • the dosage may also be, for example, about 1 to 12 mg, or about 1 to 10 mg, or in one embodiment about 1 to 5 mg.
  • the dosage may be adjusted depending on the surgical procedure.
  • the ⁇ -blocker such as propranolol
  • the ⁇ -blocker in one embodiment is administered through the right or left coronary artery in a dosage of about 0.01 to 0.07 mg/kg body weight of patient, for example, 0.01 to 0.05 mg/kg, or about 0.01 to 0.04 mg/kg.
  • the total amount of propranolol administered is in one embodiment about 1 mg to 6 mg, e.g., about 1 mg to 5 mg, or, for example, about 2 to 4 mg, or about 3 mg.
  • one embodiment to induce transient reversible ventricular asystole in a patient is as follows.
  • An intracoronary injection of 0.5 to 4 mg, e.g., about 1.0 mg, of propranolol is administered by intracoronary infusion through a drug delivery catheter positioned in the right coronary artery just proximate to the AV node artery, over a time period of about 0.5-3 minutes, e.g., about 1 minute, preferably followed by a saline flush, such as a 2 mL saline flush.
  • a dosage amount of phenylephrine in the range of about 0.1 to 1.0 mg if needed may be administered to counteract any hypotension effects associated with carbachol administration. Additionally, nitroglycerine may be required in some patients to counteract the coronary vasodilator effects of systemic phenylephrine administration.
  • ⁇ -blocker where the patient is under prior therapeutic treatment with a ⁇ -blocker, lower amounts of ⁇ -blocker, or alternatively no ⁇ -blocker may be required prior to the surgical procedure.
  • overdrive suppression i.e., pacing at about 90 to 110 beats/min for about 10 seconds
  • pacing at about 90 to 110 beats/min for about 10 seconds may be used in addition to the initial intracoronary bolus of carbachol and propranolol to initiate ventricular asystole prior to carbachol continuous infusion.
  • Compositions may be administered by intravenous, intracoronary and intraventricular administration in a suitable carrier.
  • Compositions may be administered locally to the heart, for example, by direct infusion to the right coronary artery as a single bolus injection, continuous infusion, or combination thereof. This can be achieved, for example by administration to the proximal or ostial portion of the right coronary artery, using a guiding catheter or drug delivery catheter, or by administration just proximal to the AV node artery by means of a drug delivery catheter positioned in the right coronary artery. Intraventricular (left side) injection also may be used. Continuous infusion can be continued as long as necessary to complete the procedure.
  • the infusion rate can range from about 0.01 to 0.5 mg-min -1 , e.g., about 0.01 to 0.3 mg-min -1 , or about 0.015 to 0.15 mg-min -1 , for example about 0.016 to 0.12 mg-min -1 .
  • Methods of administration include intravenous, intra-atrial, intra-aortic, and administration via the aortic root, or coronary artery. Administration may be via any suitable route, for example via the left or right ventricle, for example proximal to the AV node artery, or via the aorta, pulmonary artery, pulmonary vein, middle cardiac vein, right atrium or the coronary sinus. In another embodiment, administration may be by direct administration into the AV node artery or AV node. In one embodiment, administration may be via a hypodermic needle to the AV node.
  • systemic delivery routes of administration known in the art may be used, such as oral, transdermal, intranasal, suppository and inhalation.
  • the ⁇ -blocker may be administered orally in a suitable carrier for oral administration.
  • the patient also may be on therapeutic treatment with a ⁇ -blocker prior to the surgical procedure and thus may require lower amounts, or even no additional ⁇ -blocker prior to the surgery.
  • composition capable of inducing ventricular asystole may be provided in pharmaceutically acceptable carriers including diluents.
  • carriers may be used that are known in the art, preferably in sterile form. Suitable carriers include sterile water, aqueous normal saline solutions, and aqueous solutions such as lactated Ringer's solution, or a solution of a sugar such as dextrose, for example 5% dextrose in water or saline.
  • aqueous solutions include sodium citrate, citric acid, amino acids, lactate, mannitol, maltose, glycerol, sucrose, ammonium chloride, NaCl, KCl, CaCl 2 , sodium lactate, and sodium bicarbonate.
  • the carrier may be D5W, a solution of 5% dextrose in water.
  • Other carriers include buffered aqueous solutions, such as an acqueous solution comprising 5 mM HEPES (N-[2-hydroxyethyl)piperazine-N'-[2-ethanesulfonic acid]).
  • Antioxidants or preservatives such as ascorbic acid also may be provided in the compositions.
  • Carriers known in the art for example, for injection, oral delivery, delivery via a suppository, transdermal delivery and inhalation also may be used.
  • compositions which include an AV node blocker, such as a cholinergic agent and ⁇ -blocker either together or separately in a pharmaceutically acceptable carrier.
  • containers containing unit dosage forms of the AV node blocker, such as a cholinergic agent and the ⁇ -blocker, either in separate containers or in a single container are provided.
  • unit dosage forms of carbachol and propranolol are provided either in separate containers or in a single container for administration to a patient, optionally in combination with a pharmaceutically acceptable carrier.
  • carbachol can be present in a pharmaceutically acceptable carrier in a dosage form for administration to a patient in an amount of about 5 to 150 ⁇ g/kg body weight of the patient, or in a total amount of from about 1 to 20 mg, or in a total amount of about 5 to 10 mg.
  • the propranolol can be present in a pharmaceutically acceptable carrier in a dosage form for administration to a patient in an amount of about 0.01 to 0.07 mg/kg body weight of the patient, or in a total amount of about 1 to 10 mg, or in a total amount of about 1 to 5 mg.
  • Carbachol is available commercially from Sigma Chemical Company, St. Louis, Mo.
  • a composition comprising an AV node blocker or a ⁇ -blocker, or a combination thereof, in a pharmaceutically acceptable carrier.
  • the composition may be provided for example as an aqueous solution, or in the form of a suspension or emulsion.
  • the composition may include a mixture of AV node blockers and/or a mixture of ⁇ -blockers.
  • the composition may be provided in a form suitable for parenteral administration.
  • the composition comprises water
  • the water is preferably processed, for example by compression distillation, to ensure that it is sufficiently purified to be suitable for parenteral administration.
  • compositions of a quality suitable for parenteral administration are disclosed for example, in Gennaro, "Remington: The Science and Practice of Pharmacy,” Mack Publishing Co., Easton, Pa., 1995, Vol. 2, Chapter 87, the disclosure of which is incorporated herein.
  • the composition is provided in a form suitable for administration to the cardiovascular system during a surgical procedure.
  • the AV node blocker is a cholinergic agent.
  • the AV node blocker is carbachol.
  • the pharmaceutically acceptable composition comprising the AV node blocker or ⁇ -blocker, or combination thereof, may be provided, for example in an aqueous solution, in a container, such as a vial, it a concentration suitable for direct administration to a patient, or may be diluted, for example with saline.
  • a pharmaceutically acceptable composition comprising an AV node blocker, such as cholinergic agent, is provided, which may be used to permit local cardiac administration of the AV node blocker.
  • a pharmaceutically acceptable composition comprising carbachol, wherein the composition is suitable for parenteral administration.
  • the carrier is suitable for intracoronary administration.
  • the carbachol may be provided in an aqueous carrier, such as water.
  • the concentration of carbachol may range, for example, from about 0.01 mg/mL to 2.55 mg/mL, e.g., about 0.1 to 1.0 mg/mL.
  • the composition may further comprise a ⁇ -blocker, such as propranolol, at a concentration, for example, of about 0.5 to 6 mg/mL, for example about, 0.5 to 3 mg/mL, or, e.g., about 1.0 to 2.0 mg/mL or about 1.0 mg/mL. If needed, the composition may be diluted to a concentration suitable for local administration to the heart, e.g., via an intracoronary bolus or infusion.
  • a ⁇ -blocker such as propranolol
  • compositions also are provided including an AV node blocker, such as a cholinergic agent and/or a ⁇ -blocker that are suitable for direct local cardiac administration.
  • an AV node blocker such as a cholinergic agent and/or a ⁇ -blocker that are suitable for direct local cardiac administration.
  • a pharmaceutically acceptable composition comprising carbachol, wherein the composition is suitable for direct local administration, for example, to a coronary vessel such as the right coronary artery.
  • the carbachol is, for example, provided in an aqueous carrier, such as water.
  • the carbachol is provided in physiologic saline.
  • the concentration of carbachol may range, for example, from about 0.001 to 2.55 mg/mL, for example, about 0.01 to 2.5 mg/mL, or about 0.05 to 1.0 mg/mL, e.g., about 0.01 to 0.5 mg/mL, for example, about 0.05 mg/mL to 0.2 mg/mL, or e.g., about 0.1 to 0.2 mg/mL, or about 0.075 mg/mL.
  • the composition may optionally further comprise a ⁇ -blocker, such as propranolol, at a concentration, for example, of about 0.05 to 6.0 mg/ml, for example, 0.05 to 3.0 mg/ml, or, e.g., about 1.0 to 2.0 mg/ml, or about 1.0 mg/mL.
  • a ⁇ -blocker such as propranolol
  • the composition is suitable without dilution for local administration to the heart, e.g., via an intracoronary bolus or infusion.
  • a surgical kit including a container comprising a dosage of a cholinergic agent, such as carbachol.
  • a surgical kit includes a first container comprising a cholinergic agent and a second container comprising a ⁇ -blocker, wherein in one preferred embodiment, the cholinergic agent is carbachol and the ⁇ -blocker is propranolol.
  • the containers may include respectively a preferred dosage form of the carbachol and of the propranolol.
  • the first container may include a carbachol in a pharmaceutically acceptable carrier, and the second container may include propranolol in a pharmaceutically acceptable carrier.
  • the cholinergic agent and the ⁇ -blocker may be provided in a single container, optionally in combination with a pharmaceutically acceptable carrier.
  • the kit may further include epicardial or endocardial pacing electrodes or any other disposable items associated with the pacemaker.
  • the kit also may include a drug delivery catheter and associated disposable items.
  • the pacing system generally includes pacer, a switch box and an actuator, which preferably can be readily controlled by the physician to remotely control the pacer through the switch box.
  • the pacing system will be described with reference to the example illustrated in FIG. 1. However, it should be understood that other configurations may be used.
  • the illustrative system generally includes a pacer 18, a switch or control box 14, and an actuator, such as actuator 22 or 24.
  • Pacer 18 may be a conventional ventricular demand pacer or dual chamber (atrial-ventricular) pacer.
  • Leads 16 couple the output of pacer 18 to switch box 14 and leads 12 couple switch box 14 to the patent's heart. The latter may be achieved for example, either endocardially or epicardially.
  • Switch or control box 14 preferably is configured so that when actuated, it delivers the pacing signals or output of pacer 18 to leads 12.
  • Conductor or lead 20 couples remote actuator 22 to switch box 14.
  • the leads may be transvenously delivered for coupling to the heart.
  • electrodes such as transarterial electrodes, can be incorporated into the drug delivery catheter.
  • This pacing system of the present invention preferably provides to the surgeon remote control of the on/off pacing function only. All other parameters which are user selectable (rate, output, etc.) preferably are not remotely programmable but must be adjusted by using controls on the pacemaker.
  • Switch box 14 includes an electrical or mechanical switch 23 to which actuator 22 couples. This coupling allows the switch to be energized or deenergized as would be apparent to one of ordinary skill.
  • foot pedal 22 is configured to be in an "Off" (electrically open) position when in its normal state and to be in an "On” (electrically closed) position to open switch 23 in switch box 14 and interrupt delivery of pacing signals to the heart when the pedal is depressed. Accordingly, if the power source to the pedal is interrupted, the heart will be paced.
  • the foot pedal may be configured to be in an "On" position when in its normal state and to be in an "Off” position when the pedal is depressed.
  • switch box 14 preferably is configured in a manner to allow the pacing signal to pass through the box, to leads 12 and, thus, to the patient while actuator 22 is in the "Off" position.
  • the switch box's switch 23 opens when the actuator is activated (e.g., the foot pedal is depressed). This opening prevents the pacing signal from going to the patient.
  • the switch box's switch 23 closes to again allow the pacing signal to pass through to the patient, when the actuator is released.
  • Commercially available switch boxes and foot pedal actuators may be used.
  • a suitable switch box with foot pedal is the Treadlight 2, Catalogue No. T-91-S manufactured by Line Master Switch Corporation. This switch provides an open circuit when actuated as shown in FIG. 1A.
  • Safety features may be incorporated into the switch box.
  • the first is a timer or override circuit, either programmable or factory set, that limits the time the switch or control box can interrupt the pacer.
  • This circuit overrides the actuator, if the actuator should happen to be held down (i.e. in the "On" position) too long, i.e., longer than the preset maximum time.
  • the override circuit may be set or configured to override the activator alter an interval of time of about 0. 1-60 seconds, more preferably about 5-30 seconds, or more preferably about 10-15 seconds.
  • a second safety feature is an indicator (visual and/or audible) that indicates the pacing signal is not being sent to the patient.
  • a third safety feature is an indicator (visual or audible) that the pacing signal is going out from the control box to the patient, especially to signify the end of an interruption period (resumption of pacing).
  • the indicator or indicators are audible signals.
  • the control box could have additional features that may be more useful for the user than for safety.
  • the first feature would be an indicator, preferably audible, preparing the user for the resumption of pacing. This could be a beeping tone that increases in frequency as the interruption period ends.
  • the control panel should be battery powered either by a disposable or re-chargeable battery.
  • Other features include a control box that is preferably within 7" ⁇ 10" ⁇ 5", lightweight, less than 3 pounds, and easy to use with current pacer and pacing lead designs.
  • FIG. 1C presents one embodiment of the control box as schematically shown in FIGS. 1, 1A and 1B.
  • a suitable control box 14' includes debounce circuit 100, pull-down resistor 102, timer select switch 104, first timer 106, second timer 108, diodes 110, transistor 112, inductive solenoid coil 114, switches 116, beeper control 118, volume control 120, and speaker 122.
  • Control box 14' uses debounce circuit 100 to generate a steady signal when mechanical foot pedal 22 is depressed.
  • Debounce circuit 100 has an input terminal 100A and an output terminal 100B. The input terminal connects to pull-down resistor 102. This terminal also connects to the foot pedal switch 22A of foot pedal 22.
  • the foot pedal switch When the foot pedal switch is open as shown in FIG. 1C (e.g., when the operator does not depress the foot pedal), the input terminal is pulled to ground through pull-down resistor 102.
  • the foot pedal switch closes (e.g., when the operator depresses the foot pedal)
  • the input terminal connects to the power supply voltage source through the foot pedal switch 22 in order to receive the power supply voltage.
  • the debounce circuit In response to the power supply voltage provided by mechanical foot pedal 22, the debounce circuit generates a signal on its output terminal that it steadily maintains at one level (e.g., the ground level) until the foot pedal switch opens.
  • the output terminal 100B of the debounce circuit 100 connects to first timer 106.
  • the voltage on this output terminal is usually in a first level (e.g., the power supply voltage) when the input to the debounce circuit is pulled to ground (i.e., when the foot pedal has not been depressed).
  • this output terminal's voltage transitions to a second level (e.g., the ground voltage) when the input to the debounce circuit transitions to the power supply voltage (i.e., when the foot pedal has been depressed).
  • the voltage at the output terminal 100B in combination with the signal supplied to the reset pin 106C of the first timer circuit controls the operation of this timer circuit.
  • Control box 14' uses first and second timer circuits 106 and 108 in order to measure the lapse of a selected period of time.
  • the amount of time selected on time select rotary switch 104 is the maximum amount of time that the physician can interrupt the supply of the pacing signal to the heart by depressing the foot pedal.
  • the control box 14' determines, through the use of timers 106 and 108, that the maximum amount of time has expired, then the control box 14' overrides (i.e., ignores) the signal generated by the depressed foot pedal and resumes the supply of the pacing signal to the patient.
  • the second timer counts the last five seconds in the selected period of time, while the first timer counts the remainder of time.
  • Both the timers 106 and 108 have reset pins (i.e., reset terminals) 106A and 108A that receive the signal supplied to input terminal 100A of debounce circuit 100.
  • reset pins i.e., reset terminals
  • the timer enters its reset mode and resets its measured time value to its initial value.
  • Each timer exits its reset mode and enters a standby mode when the signal supplied to its reset terminal is high (i.e., when the foot pedal has been depressed).
  • each timer enters its operational modes when it receives a trigger signal at its input after it has entered its standby mode. Once the timers are in their operational modes, they start counting up or down to their expiration values when they receive an appropriate signal (e.g., a high voltage) on their input terminals 106A, 108A.
  • First timer 106 receives its trigger signal from the output of the debounce circuit.
  • the transition of the output of the debounce circuit from one state to another e.g., goes from a high level to a low level
  • the first timer 106 starts to count towards its expiration value.
  • the physician determines the expiration value of the first timer by operating the timer select switch 104, which connects to the first timer.
  • the signal at this timer's output terminal 106B is at a first voltage level (e.g., the power supply level).
  • the signal from output terminal 106B flows through diode 110A and is supplied to the gate of transistor 112 to turn ON this transistor.
  • Transistor 112 can be any type of transistor. In FIG. 1C, this transistor is an NMOS device.
  • transistor 112 When transistor 112 turns ON, it draws current from the power supply through the inductive solenoid coil 114.
  • This coil serves as a relay (i.e., coil that when energized operates a mechanical switch).
  • the solenoid coil When current passes through the solenoid coil, it activates the relay which opens switches 116A-D of patient connect relay 124.
  • switches A-D couple the signal from the pacer to the patient through leads 12.
  • switch 116A couples a ventricle inlet (V-IN(-)) to a ventricle outlet (V-OUT(-)).
  • Switch 116B couples a ventricle inlet (V-IN(+)) to a ventricle outlet (V-OUT(+)).
  • Switch 116C couples an atrial inlet (A-IN(-)) to an atrial outlet (A-OUT(-)), while switch 116D couples an atrial inlet (A-IN(+)) to an atrial outlet (A-OUT(+)).
  • the inlets are coupled to the pacer and the outlets are coupled to the patient. Referring to FIG.
  • FIG. 1D a schematic representation of an endocardial lead arrangement between the control box and the right atrium of a patient is shown, together with the coupling between the control box and the pacer.
  • An actuators may be coupled to the control box as described above.
  • the inlets (A-IN(-), A-IN(+)) may be coupled to the pacer 18 adapter cables and the outlets (A-OUT(-), A-OUT(+)) may be coupled to the patient with leads as shown in the drawing and as would be apparent to one of ordinary skill.
  • one lead may be coupled to positive terminal 140, which is in the form of a ring, and the other lead may be coupled to a negative terminal 142, which may have a generally hemispherical configuration.
  • a similar arrangement can be used to couple the control box to the right ventricle.
  • epicardial leads as shown in FIG. 1E may be preferred.
  • epicardial leads which may be sutured to the heart (e.g., right atrium) as shown in FIG. 1E and generally designated with reference character "S", generally are preferred in open chest procedures since they can be readily sutured to the heart.
  • a similar arrangement can be used to couple the control box to the right ventricle.
  • patient connect relay 124 is shown as a dual chamber pacing system, it should be understood that single chamber pacing systems can be used to pace the ventricle as would be apparent to one of ordinary skill in the art (e.g., by only using switches 16A and B shown in FIG. 1C).
  • the output of the first timer is also supplied to a beeper control circuit 118, which controls the output of a speaker 122.
  • a beeper control circuit 118 which controls the output of a speaker 122.
  • the signal at its output terminal transitions from the first voltage level to a second voltage level (e.g., transitions from the power supply level to ground level).
  • the first timer then enters its standby mode, where it will stay until it is reset by the opening of the foot pedal switch.
  • the second timer has an edge detector (e.g., a negative edge detector) that detects this transition. Once it detects this transition, the second timer transitions into its operation mode, and thereby starts to count towards its expiration value.
  • the second timer's expiration value is set at five seconds.
  • the signal at its output terminal is at a first voltage level (e.g., the power supply level).
  • diode 110B supplies this signal to the gate of transistor 112, and thereby keeps this transistor ON. While transistor 112 is ON, it continues to draw current through the coil 114, which, in turn, keeps switches 116A-D, which control delivery of the pacer signal to the patient, open.
  • the output of the second timer is also supplied to a beeper control unit.
  • this output when this output is active (i.e., its at a first voltage level, such as the power supply level), it turns ON the beeper control unit, which in turn generates a second audible signal through speaker 122.
  • the output of the timers resets to the second voltage level (e.g., ground) whenever the foot pedal switch opens and the timers are reset. This resetting operation overrides the counting operation of the timers. Thus, if the timers are in the process of counting, the opening of the foot pedal makes these timers stop counting and reset. Any suitable timers may be used such as 555 timers manufactured by National Semiconductor (Santa Clara, Calif).
  • a conventional needle holder 24 can be used to control the pacer switch box.
  • the needle holder preferably is of the standard Castro-Viejo variety.
  • any other manual switch actuator operable by the surgeon for opening and closing the switch in switch box 14 on demand can be used in accordance with the invention to electrically connect and disconnect pacer 18 with pacing leads 12.
  • the actuator can be incorporated in or on one of the surgeon's instruments, such as surgical site retractor, or any other location easily and quickly accessed by the surgeon.
  • Any conventional pacer suitable for ventricular demand pacing and having external leads that can be electrically coupled to a switch box 14 may be used.
  • An example of such a suitable pacer is the Medtronic model 5330 or 5375, Demand Pulse Generator manufactured by Medtronic Inc. (Mpls, Minn.)
  • pacer and switch box may be combined in a single unit.
  • specifications of the pacemaker should be similar to currently manufactured external pacemakers (e.g., Ventricular or atrial-ventricular sequential; Rate range: 30 to 180 ppm (pulses per minute), continuously adjustable or in increments of 1 ppm; Output current range: 0.1 to 20 mA; Sensitivity range: 1.0 mV(maximum) to asynchronous; Pulse width: 1.8 ms maximum).
  • Pacer 18 preferably is an extracorporeal pacer and differs from implantable pacemakers in the following ways. Pacer 18 typically will be in excess of 400 grams, can use replaceable (battery life of approximately 500 hours) or rechargeable batteries (9 v), may be line power designed to last several years, and need not be constructed with a biocompatible exterior shell or be hermetically sealed.
  • the pacing system may be configured to synchronize activation and deactivation of the patient's ventilator (not shown) with pacing.
  • the control box may be configured for coupling to a ventilator so that pacing and ventilator signals are simultaneously delivered to the patient leads 12 and the ventilator when the actuator is in a first state (e.g., when the foot pedal is released).
  • the pacing and ventilator signals are simultaneously interrupted when the actuator is in a second state (e.g., when the foot pedal is depressed).
  • the synchronization of pacing with a ventilator may minimize or eliminate unwanted heart motion associated with a patient's breathing with a ventilator.
  • FIGS. 2-7 show delivery into the coronary sinus (FIG. 4 shows an alternative balloon configuration);
  • FIG. 5 shows intra-aortic delivery; and
  • FIGS. 6 and 7 show delivery through the right coronary artery. Discussion of a further delivery procedure in accordance with the present invention, intraventricular injection, also will be provided.
  • Coronary sinus delivery catheter 30 is shown for local drug administration into the coronary sinus (CS) according to the present invention.
  • Coronary sinus delivery catheter 30 preferably is a medium-diameter, e.g. about 6-8 French, single or dual lumen, flexible catheter.
  • the tip of catheter 30 may be curved slightly to give a so-called hockey-stick appearance as shown in the drawings. This configuration facilitates, for example, introducing the catheter into the coronary sinus from the atrium as shown in FIG. 2 where the distal tip is shown prior to introduction into the coronary sinus.
  • a low-pressure balloon 32 of up to about 2 cm in diameter is located near the tip of the catheter.
  • catheter 30 further includes inflation lumen 37 and drug delivery lumen 39 (FIGS. 2A and 3A) which fluidly couple ports 34 and 36 to balloon 32 and delivery or discharge opening 38.
  • any of three catheter lengths may be used depending on whether the catheter is introduced into the coronary sinus: (A) through the right atrium or atrial appendage; (B) via the internal jugular or subclavian vein; or (C) via the femoral vein.
  • a guidewire (not shown) is used to facilitate transvenous placement, and a stiffer wire obturator (not shown) is provided for catheter insertion through the right atrial appendage.
  • Access to the right atrial appendage requires an operative approach through the right chest or through the mediastinum.
  • a plegeted pursestring suture e.g. 4/0 polypropylene
  • RA right atrium
  • catheter 30 is secured in place with a Rumel-tourniquet.
  • the transvenous approaches (approaches B and C) require expertise in coronary sinus cannulation over a guidewire using fluoroscopic or echocardiographic guidance.
  • the internal jugular or subclavian approach accesses the coronary sinus via the superior vena cava (SVC) as shown in FIG. 2.
  • the femoral vein approach accesses the coronary sinus via the inferior vena cava (IVC).
  • the guidewire or obturator which was used to introduce the catheter into the coronary sinus, is removed.
  • Injection port 36 is then connected to a three-way stopcock (not shown) for intermittent measurement of coronary sinus pressure and administration of the composition(s) provided in accordance with the present invention.
  • a right ventricular pressure wave form is observed.
  • the inventive composition(s) is then administered as a bolus injection through drug injection port 36 so as to be delivered at the delivery port 38.
  • Coronary sinus pressure during bolus injection generally should not exceed about 30 mm Hg.
  • the composition(s) may be administered as a bolus injection followed by continuous infusion or as a continuous infusion alone.
  • Balloon inflation may be rapid inflation/deflation balloon synchronized with the electrocardiogram (ECG).
  • ECG electrocardiogram
  • the coronary sinus may be occluded, partially or completely, for a period of about one or two hours.
  • Balloon 32 may have a much thinner wall construction than balloon 42 (discussed below) because it need not expand against arterial pressure.
  • Previously placed pacing leads 12 permit ventricular pacing during drug induced ventricular asystole. Removal of the catheter simply requires deflation of the balloon and closure of the atriotomy with the pursestring suture.
  • Catheter 30' is provided with laterally spaced balloons 32' which are fluidly coupled to inflation lumen 39'.
  • Drug delivery lumen 37' opens in a region between the balloons.
  • Another drug administration approach is intraventricular injection into the left ventricle via a catheter (not shown).
  • the catheter may be delivered in retrograde fashion through the arterial system, aorta and through the aortic valve into the left ventricle.
  • a catheter or cannula may be inserted directly into the left ventricle (preferably the apex) through a hole made by the surgeon.
  • a needle may be inserted directly into the left ventricle.
  • Catheter 40 preferably is a dual lumen catheter provided for rapid inflation and deflation of a durable, low-pressure balloon 42 arranged to inflate in synchronization with heart beat (e.g., electronically synchronized with ECG "P" waves so that balloon 42 inflates during diastole and deflates just before systole).
  • heart beat e.g., electronically synchronized with ECG "P" waves
  • a balloon inflation port 44 and a drug injection port 46 are provided.
  • Catheter 40 a drug delivery and inflation lumens similar to catheter 30 with the exception that the drug delivery lumen in catheter 40 terminates with a discharge opening 48 proximal to balloon 42 this configuration facilitates delivery of drugs in the vicinity of the coronary arteries.
  • Catheter 40 may be inserted through a hole made by the surgeon in the wall of the aorta as shown in FIG.
  • catheter 30 or 30' for example, is preferred.
  • the balloon diameter may be larger to correspond with the larger size of the aorta and the balloon walls also may be constructed to withstand the greater pressures in the aorta.
  • a pursestring suture (not shown) is placed on the aortic root and catheter 40 is inserted into the ascending aorta and secured with a Rumel tourniquet.
  • the intra-aortic balloon is inflated during diastole and deflated during systole, using the patient's ECG signal for synchronization.
  • Drug delivery is given with a bolus infusion and/or continuous infusion.
  • drug induced ventricular asystole the heart is electrically paced, as detailed herein below, permitting continued intra-aortic counterpulsation.
  • catheter 40 is removed after the distal anastomosis is completed. Then, a partially occluding clamp is placed on the aorta, and the aortitomy may be used for the proximal aortosaphenous anastomosis. Alternatively, the catheter 40 may be removed and the aortic pursestring simply tied.
  • Another drug administration approach is direct infusion into the right coronary artery (RCA). This approach advantageously delivers drug more local to the AV node than the approaches described above. Other methods are generally less efficient because when mixed in the aorta, ventricle, or other parts of the cardiovascular system, significant drug dilution occurs by the time it reaches the AV branch of the RCA.
  • This approach can be achieved by either injection into the proximal or ostial portion of the RCA, by use of a guide catheter or drug delivery catheter, or by injection just proximal to the branch perfusing the AV node (AV node artery) by means of a drug delivery catheter positioned in the RCA as shown in FIG. 6.
  • the drug delivery catheter can be positioned directly in the AV node artery through the RCA to delivery the drug more locally to the AV node.
  • the catheter may be introduced into the coronary artery via the arterial system (femoral, radial, subclavian) with a larger diameter coronary guiding catheter.
  • the catheter may be used in a similar fashion to deliver the drug into the left coronary artery to, for example, the circumflex branch.
  • Catheter 50 is a small diameter (for example, about 3-4 French) single lumen catheter with a drug delivery opening 58 located at the distal end of the catheter to provide selective coronary artery drug delivery.
  • catheter 50 maximizes the volume of catheter lumen dedicated to drug delivery while minimizing catheter diameter.
  • catheter 50 is introduced into the right coronary artery under flouroscopic guidance through a larger diameter (6-8 French) coronary guiding catheter 56, which is positioned at the ostium, and over a guidewire which is placed distally in the RCA.
  • a larger diameter (6-8 French) coronary guiding catheter 56 which is positioned at the ostium, and over a guidewire which is placed distally in the RCA.
  • the guiding catheter is pulled back from the ostium of the RCA to provide blood flow to the RCA, the guidewire is removed, and a bolus dose is given.
  • a continuous infusion of drugs can be administered into the distal right coronary artery.
  • Coronary catheter 50 is small enough that blood flow is not significantly impeded to the RCA.
  • Catheter 60 is the same as catheter 50 with the exception that catheter 60 has a bent distal end portion 62.
  • Catheter 50 or portion 62 can be positioned within the branch (B) to the AV node.
  • the bent distal end configuration minimizes or eliminates the possibility of the catheter entering the branch going down a posterior left ventricular branch.
  • trans-epicardial absorption e.g., a trans-myocardial patch which slowly releases pharmaceutical agents into the myocardium.
  • the heart Prior to drug delivery, the heart is prepared for cardiac pacing as discussed above.
  • leads 12 may be temporarily affixed to the right ventricle of the heart such as by suturing or other manner as would be apparent to one of skill in the art.
  • Drugs are administered to the heart through, for example, any one of catheters 30, 40, 50 or 60 to induce ventricular asystole.
  • Pacing of the heart is established and maintained.
  • the pacing can be transiently interrupted by temporarily deactivating the pacemaker using, for example, foot pedal 22. When the foot pedal is in its deactuated, raised position, the switch in the pacer switch box is closed, and current flows from the ventricular demand pacer 18, through the switch box 14 and the pacing wires 12 to the heart 10 without impediment.
  • the heart preferably is paced at a rate between 90 to 110 beats/minute.
  • pacing is disabled by depressing the foot pedal. In the illustrated and currently preferred embodiment, this opens the switch in pacer switch box 14, stopping the current flow from pacer 18 to pacing leads 12. Since no current reaches the heart while the foot pedal is depressed, ventricular asystole occurs, thus allowing precise suturing or other manipulative procedures to be performed.
  • the pacer may be reactuated by releasing the foot pedal, thereby to reestablish the electrical connection between the pacer 18 and the pacing wires 12 and resuming pacing of the heart at the prescribed rate until another precise manipulation is required.
  • a surgeon-controlled device such as with a foot pedal, remote from the pacer for controlling the pacer, the surgeon can have complete and immediate control over when pacing is interrupted, even though the surgeon also has surgical instruments in his or her hands. This allows the surgeon to coordinate precisely the pacing of the heart to the manipulative step, thereby minimizing unnecessary and undesired cardiac arrest.
  • the pacer control box also may be configured to control interruption of a patient's ventilator so that the pacing may be synchronized (eg., the actuator activates pacing and ventilating equipment (not shown) simultaneously and deactivates pacing and the ventilating equipment simultaneously).
  • the switch box can be electrically coupled to a ventilator so that when the foot pedal described above is depressed pacing and ventilation are deactivated and when it is released, pacing and ventilation resume. This arrangement may eliminate some small motions of the heart associated with a patient's breathing during a surgical procedure.
  • the heart was exposed through a median sternotomy and suspended in a pericardial cradle.
  • Two temporary epicardial pacing wires were affixed to the right ventricle and connected to an external pacemaker (Medtronic, Inc., Minneapolis, Minn.).
  • the pacemaker was modified to permit deactuation by means of depressing a foot pedal.
  • an AR-1 guide (Cordis Corp., Miami Lakes, Fla.) was placed into the right coronary artery.
  • An 0.014-inch floppy guide wire was then advanced into the right coronary artery to the level of the posterior descending coronary artery.
  • the AR-1 guide was removed and a 2.5 Fr Tracker (Cordis Corp., Miami Lakes, Fla.) Catheter was inserted over the guide wire. Using dye injection, the catheter was positioned just proximal to the take-off of the atrioventricular node artery. Carbachol (Sigma St. Louis, Mo.) solution was prepared the day of the experiment and infused at a constant rate using a Harvard pump.
  • carbachol was continuously infused through the Tracker catheter at increasing doses of 0.44, 0.62, 0.88, and 1.72mg/min, until ventricular asystole was observed.
  • a 1 mg dose of propranolol (0.04-0.05 mg/kg) was administered through the Tracker catheter.
  • Carbachol was then administered as a 0.5 mg intracoronary bolus (0.02 mg/kg) followed by a constant infusion.
  • the infusion rate necessary to achieve ventricular asystole was 0.03 mg/min (1.1 to 1.2 ⁇ g/kg/min).
  • the heart was paced at 100 beats/minute. At 60-second intervals, the pacemaker was turned off for five seconds to determine the underlying cardiac rate and rhythm.
  • SBP systolic blood pressure
  • DBP diastolic blood pressure
  • MAP main arterial pressure
  • the propranolol and carbachol were used at the end of the CABG surgery only during repair of leaking distal vascular anastomoses, while the patients were still on cardiopulmonary bypass (CPB) subsequent to the removal of the aortic cross clamp.
  • CPB cardiopulmonary bypass
  • the carbachol and propranolol drugs and temporary pacing were used for the CABG procedure itself, and the aortic cross clamp was avoided.
  • the patients were selected based on the following key criteria. Patients were selected ranging between 18 and 70 years in age with a normal sinus rhythm with P-wave-R-wave interval not exceeding 0.16 sec. Men or women were selected who had a stable coronary artery disease and were undergoing elective CABG revascularization of distal target(s) in the left anterior descending (LAD) artery system, right coronary artery (RCA) and/or the left circumflex (LCX) artery.
  • LAD left anterior descending
  • RCA right coronary artery
  • LCX left circumflex
  • Patients were selected with right dominant coronary circulation or an expectation that their AV node was supplied by the RCA, and with the presence of at least two of the following angiographic criteria: (1) coronary arteries greater than 2 mm in diameter, (2) noncalcified coronary arteries, or (3) an LAD that was not intramyocardial.
  • CABG surgery was performed using well established traditional methods. Patients were placed on CPB, the aorta was cross-clamped and cardioplegic arrest was administered. After distal and (if applicable) proximal anastomoses were sutured, the cross-clamp was removed and (if necessary) the heart defibrillated with patients still on CPB. When a leak requiring repair was detected at the distal anastomotic site(s), epicardial pacemaker leads were sewn into place on the ventricles and, optionally, the right atrium, of the patients and the pacing thresholds determined and recorded. A temporary pacemaker was connected to the epicardial leads. The pacing voltage was set at 10 times the pacing threshold.
  • VVI ventricular-ventricular inhibited
  • VAT ventricular-atrial triggered
  • fluoroscopy was used to position an appropriate catheter.
  • a TrackerTM Track Therapeutics, Freemont, Calif.
  • This catheter was used for intracoronary administration of the study drugs. If at any time during the procedure, catheter displacement was noted, repeat angiography was used to reposition the catheter.
  • Adequate supplies of phenylephrine, other adrenergic agents and volume repletion fluids were available at he bedside during and following drug administration in the event of unexpected adverse events, to control blood pressure, and/or to protect against inadvertent overdose.
  • the propranolol solution used was an injectable solution of Inderal® (Wyeth-Ayerst, Philadelphia, Pa.).
  • the initial propranolol dose was 1 mg of a 1 mg/mL solution.
  • the carbachol infusion solution was prepared by adding 5 ml, of this solution to 250 mL of sterile saline. After reconstitution, the resulting concentration of the carbachol solution was 0.005%, or 0.05 mg/mL.
  • the initial dose of carbachol was 0.025 mg or 0.5 mL and the initial infusion rate was 0.025 mg/min or 0.5 mL/min of the 0.005% solution.
  • Carbachol was administered as an intracoronary low dose bolus and as an infusion.
  • the bolus dose of carbachol used to initiate reversible ventricular asystole was in the range of 0.05-0.225 mg and the sustained infusion of carbachol used to maintain ventricular asystole was in the range of 0.05-0.15 mg/min.
  • overdrive pacing was used in conjunction with the loading dose of carbachol to induce ventricular asystole.
  • the drugs and temporary pacing were used for the CABG procedure itself.
  • a loading dose of 4 mg propranolol and 0.15 mg of carbachol were administered via intracoronary delivery to Patient 201 to initiate reversible ventricular asystole.
  • an infusion of carbachol at a rate of 0.1 mg/min was given via intracoronary delivery to the patient to maintain ventricular asytole for a period of about 45 minutes.
  • a dose of phenylephrine ranging between about 0.24-0.80 mg was administered to Patients 101, 103, 105-109 and 201 to control hypotension.
  • the drug infusion was stopped and atropine was administered to determine the reliability of pharmacologic reversal of complete heart block with the exception of Patient 201, who was allowed to return to normal sinus rhythm naturally, over less than 15 minutes.
  • the dosage amount of atropine used to reverse arrest in Patients 101-108 was about 1.0 mg.
  • CPB was removed. Established procedures for closing of the chest were followed.
US09/131,075 1997-08-08 1998-08-07 Compositions, apparatus and methods for facilitating surgical procedures Expired - Lifetime US6060454A (en)

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US09/131,075 US6060454A (en) 1997-08-08 1998-08-07 Compositions, apparatus and methods for facilitating surgical procedures
US09/379,381 US6087394A (en) 1997-08-08 1999-08-23 Compositions, apparatus and methods for facilitating surgical procedures
US09/382,705 US6141589A (en) 1997-08-08 1999-08-23 Switch control for external pacing system
US09/379,179 US6127410A (en) 1997-08-08 1999-08-23 Compositions, apparatus and methods for facilitating surgical procedures
US09/379,180 US6043273A (en) 1997-08-08 1999-08-23 Compositions, apparatus and methods for facilitating surgical procedures
US09/406,333 US6711436B1 (en) 1997-08-08 1999-09-27 Compositions, apparatus and methods for facilitating surgical procedures
US09/469,956 US6101412A (en) 1997-08-08 1999-12-21 Compositions, apparatus and methods for facilitating surgical procedures
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US09/379,381 Division US6087394A (en) 1997-08-08 1999-08-23 Compositions, apparatus and methods for facilitating surgical procedures
US09/382,705 Division US6141589A (en) 1997-08-08 1999-08-23 Switch control for external pacing system
US09/406,333 Continuation-In-Part US6711436B1 (en) 1997-08-08 1999-09-27 Compositions, apparatus and methods for facilitating surgical procedures
US09/469,956 Continuation US6101412A (en) 1997-08-08 1999-12-21 Compositions, apparatus and methods for facilitating surgical procedures
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US09/379,180 Expired - Lifetime US6043273A (en) 1997-08-08 1999-08-23 Compositions, apparatus and methods for facilitating surgical procedures
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US09/382,705 Expired - Lifetime US6141589A (en) 1997-08-08 1999-08-23 Switch control for external pacing system
US09/469,956 Expired - Lifetime US6101412A (en) 1997-08-08 1999-12-21 Compositions, apparatus and methods for facilitating surgical procedures
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US09/379,381 Expired - Lifetime US6087394A (en) 1997-08-08 1999-08-23 Compositions, apparatus and methods for facilitating surgical procedures
US09/382,705 Expired - Lifetime US6141589A (en) 1997-08-08 1999-08-23 Switch control for external pacing system
US09/469,956 Expired - Lifetime US6101412A (en) 1997-08-08 1999-12-21 Compositions, apparatus and methods for facilitating surgical procedures
US09/494,145 Expired - Lifetime US6414018B1 (en) 1997-08-08 2000-01-28 Compositions, apparatus and methods for facilitating surgical procedures

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US6101412A (en) 2000-08-08
US6414018B1 (en) 2002-07-02
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EP1051168B1 (en) 2006-03-01
ATE318595T1 (de) 2006-03-15
WO1999007354A3 (en) 1999-04-29
US6127410A (en) 2000-10-03
US6141589A (en) 2000-10-31
US6087394A (en) 2000-07-11
AU9015698A (en) 1999-03-01
CA2300049A1 (en) 1999-02-18
US6043273A (en) 2000-03-28
JP2001513495A (ja) 2001-09-04
WO1999007354A2 (en) 1999-02-18

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